Molecular detection and risk factors for Anaplasma platys infection in dogs from Egypt

Background Anaplasma platys is a tick-borne bacterium which infects blood platelets of dogs, causing canine cyclic thrombocytopenia. The disease is distributed worldwide, particularly in the tropics and subtropics, but information on the epidemiology of A. platys infection in dogs is fragmentary in many countries, including Egypt. In this study, we investigated the prevalence and risk factors associated with A. platys infection in dogs from Egypt. Methods A conventional PCR targeting a fragment of the 16S rRNA gene of A. platys was used to screen 500 dogs from five North Egyptian governorates. DNA sequencing and phylogenetic analysis were performed for one of the positive samples. Results The overall prevalence of A. platys in the studied dogs was 6.4%. Females of the German shepherd breed without veterinary care had higher odds for A. platys positivity. High tick infestation and lack of anti-tick treatment were also identified as risk factors for A. platys infection. Phylogenetic analysis revealed that the sequence obtained herein was closely related to sequences from Egypt, South Africa and Uruguay. Conclusions This is the first large-scale epidemiological study of A. platys in Egypt, where female German shepherd dogs without veterinary care, as well as dogs with high tick infestation and without anti-tick treatment are at a higher risk of infection. Graphical abstract

Egypt [23]. Nonetheless, information on the epidemiology of A. platys in African countries, including Egypt, is still fragmentary. Therefore, the present study aimed to determine the molecular prevalence of A. platys infections in dogs from five governorates in northern Egypt and to evaluate the possible risk factors associated with this infection.
The study was conducted in five governorates, including Cairo, Giza, Qalyubia, Gharbia and Kafr ElSheikh, situated in the North of Egypt (Fig. 1). The climatic conditions of these regions are tropical and humid with two distinct seasons: a dry season from May to September and a warm and humid season from October to April. In the dry season, the average temperature ranges between 15 °C and 28 °C; in the rainy season, the annual average rainfall is 200 mm.
The study was carried out between December 2019 and November 2020. Blood samples were collected from 500 privately owned dogs of different breeds (i.e., German shepherd, Rottweiler and pit bull). Upon physical inspection, some dogs were apparently healthy, whereas others showed clinical signs suggestive of vector-borne pathogens (e.g., fever, lethargy and bleeding disorder). Sampling was done in the presence of a veterinarian and with the verbal consent of the owners. Blood samples were collected aseptically from the cephalic vein into EDTA tubes and kept at −20 °C until further processing. Data about sex, age, breed, tick infestation, anti-tick treatment and veterinary care were recorded and analyzed as possible risk factors.
For molecular analysis, genomic DNA was extracted from 200 µl whole blood sample of each dog using the QIAamp DNA Mini Kit ® (Qiagen, Valencia, USA) following the manufacturer's instructions. A conventional polymerase chain reaction (PCR) assay targeting the 16S rRNA gene was performed as previously described [24], using the primers PLATYS (GAT TTT TGT CGT AGC TTG CTATG) and EHR16SR (TAG CAC TCA TCG TTTAC AGC), which produce an amplicon of 678 base pairs (bp). PCR was performed in a 25 µl volume, containing 1 µl of each primer (20 pmol/μl), 12.5 µl of DreamTaq Green PCR Master Mix (2×) (Thermo Scientific, Germany), 5.5 µl nuclease-free water and a 5 µl aliquot of isolated DNA. The thermal profile of the PCR was as follow: 95 °C for 5 min followed by 40 cycles of denaturation at 95 °C for 30 s, annealing at 55 °C for 30 s and extension at 72 °C for 90 s, and final extension of 72 °C for 5 min. The amplification products were visualized on a 2% agarose gel with ethidium bromide under UV light. The PCR product of a positive sample was purified using the QIAquick PCR Purification Kit (QIAGEN, Valencia, CA, USA) and sequenced using the same primers as the conventional PCR assay. The sequencing was performed in a 3500 Genetic Analyzer (Applied Biosystems, USA) using the BigDye ™ Terminator v3.1 Cycle Sequencing Kit (Applied Biosystems, USA) according to manufacturer's protocol. The sequences obtained were assembled and edited using the BioEdit program and deposited in GenBank under accession number LC632659. The obtained sequence was aligned with other Anaplasmataceae 16S rRNA gene sequences retrieved from GenBank using CLUSTAL W (http:// www. clust alw. genome. jp). A phylogenetic tree was constructed using the neighbor-joining tree method with 1000 bootstrap replicates based on the Kimura 2-parameter model for nucleotide sequences using MEGA7 [16].
The data were analyzed using SPSS software (version 24.0, IBM Corp., Armonk, NY USA). Univariate and multivariate logistic regression analyses were used to evaluate the potential risk factors for A. platys infection. The odds ratios (OR), P-values (≤ 0.05) and 95% confidence intervals (95% CI) were evaluated to determine the strength of association between variables. A P-value ≤ 0.05 was considered significant. Analyzed risk factors included locality (Cairo, Giza, Qalyubia, Gharbia and Kafr El Sheikh), sex, age group (< 2, 2-5, and > 5 years), breed (German shepherd, Rottweiler and pit bull), tick infestation, antitick treatment and veterinary care.
In the univariate analysis, the prevalence of A. platys was higher in female dogs and German shepherd breed ( Table 1). The risk of infection with A. platys was significantly associated with lack of veterinary care, tick infestation and lack of anti-tick treatment (Table 1). In the multivariate logistic regression, A. platys infection was significantly associated with female sex, German shepherd breed, tick infestation, lack of veterinary care and lack of anti-tick treatment ( Table 2).
The obtained 16S rRNA gene sequence showed nucleotide identity > 99% with other A. platys sequences from GenBank (MZ068099, MT053461, MT044313, MT044313) using BLAST. Phylogenetic analysis was performed using a 423 bp fragment of the A. platys 16S rRNA gene generated herein along with 21 A. platys sequences available in GenBank. The phylogenetic tree demonstrated that the sequence obtained herein is closely related to a sequence from Egypt (GenBank: MZ068099) and formed a cluster with other sequences from South Africa and Uruguay (Fig. 2). Nonetheless, additional data from a larger number of sequences are necessary for understanding the clinical-epidemiological significance (if any) of this phylogenetic finding.
Overall, the prevalence of A. platys in dogs in Egypt found herein (i.e., 6.4%) is similar to that reported in Argentina [17], and slightly higher than that reported in some studies in Italy [18], Croatia [19] and Mexico [20]. On the other hand, the prevalence found herein is lower than that reported in other studies conducted in Paraguay [30], Brazil [21], French Guiana [22] and Chile [23]. In Africa and Asia, previous studies were performed in different countries such as Algeria [12], Nigeria [24], South Africa [25], Malaysia [26], Iran [27] and Turkey [28], where the reported prevalence of A. platys infection ranged between 4.4 and 13.3%. These differences in the prevalence of A. platys infection may be attributed to local risk factors including climate, vector density, socioeconomic factors and lack of anti-tick preventatives, but also to methodological factors.
In this study, older dogs were more likely to be positive for A. platys than juvenile dogs, as reported in previous study in Egypt [14,29]. This may be related to an increased risk of exposure during the dog's life. Interestingly, no breed, age, or sex predisposition has been described for A. platys infection in dogs in Europe [30].
The positivity to A. platys was significantly higher in females than in males, as opposed to previous studies from Egypt [14,31]. This may be related to higher tick exposure in females as compared to males in the area investigated in the present study. Concerning the breed, German shepherd dogs were more likely to be infected than other breeds, as reported previously in Egypt [14]. Again, no breed predisposition [30], or even slightly lower risk in purebred dogs [31], has been reported previously, which suggests that this apparent breed predisposition in German shepherd dogs in Egypt may be related to local factors that increase tick exposure in these dogs. Further studies on breed predisposition for A. platys infection in dogs are advocated. As expected, the absence of veterinary care and treatment against ticks were significant risk factors for A. platys infection, as reported previously [14,32].
The sequencing of the partial 16S rRNA gene showed high sequence identity with another A. platys isolate (GenBank: MZ068099) from Egypt. Furthermore, the phylogenetic analysis of the obtained A. platys strain clustered together with other reference strains of A. platys from Uruguay, South Africa and Egypt. The molecular identification of A. platys in some governorates of northern Egypt highlights the need for notification of veterinarians, dog owners and public health authorities to prevent the spread of vector-borne infections among dogs.  In conclusion, our study confirms the presence of A. platys in dogs from Egypt. The prevalence of disease was higher in females, particularly German shepherd dogs. In addition, absence of veterinary care, lack of anti-tick treatment and high tick infestation were identified as risk factors for A. platys infection in these dogs. The phylogenetic analysis confirmed the sequence identified herein with a previous Egyptian strain and other A. platys in GenBank.

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